"PreventionGenetics, part of Exact Sciences"[submitter] AND "POC1B"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 733918	NM_172240.3(POC1B):c.1433G>T (p.Ser478Ile)	LOC105369889, POC1B (S478I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 738353	NM_172240.3(POC1B):c.809C>T (p.Thr270Met)	POC1B (T270M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 1644427	NM_172240.3(POC1B):c.420G>A (p.Leu140=)	POC1B	Single nucleotide variant (synonymous variant +1 more)	POC1B-related disorder +1 more	GLikely benign
Select item 1156971	NM_172240.3(POC1B):c.196G>A (p.Val66Met)	POC1B (V24M +1 more)	Single nucleotide variant (missense variant)	POC1B-related disorder +1 more	GLikely benign
Select item 713426	NM_172240.3(POC1B):c.168T>C (p.Tyr56=)	POC1B	Single nucleotide variant (synonymous variant)	POC1B-related disorder +1 more	GBenign/Likely benign
Select item 3055128	NM_172240.3(POC1B):c.63C>T (p.Ile21=)	LOC130008356, POC1B +1 more (S108L)	Single nucleotide variant (synonymous variant +3 more)	POC1B-related disorder	GLikely benign

ClinVar